- Worked in collaboration with Principal Investigators, Sub-Investigators and staff to prepare new clinical trials to be submitted to the Institutional Review Board including but not limited to protocol, consent forms, amendments, serious adverse events, protocol violation reports, continuing review reports etc - Established and maintained regulatory files and protocol in current monitoring/audit ready condition. - Screened potential patients for eligibility through record review of laboratory rests, radiology results/films, pathology and past medical history, for criteria related to participation in clinical trials. - Coordinated patient participation in the research study. Scheduled patients for all pre-study, interim and follow up testing. - Completed all case report forms, electronic case report forms, resolves all data queries per protocol requirements. - Organize investigator’s start-up meeting and study site initiation meeting.